Canonical Allele Identifier: CA2583603011

Gene: CRLF1

Linked Data

• gnomAD v4: 19-18596538-A-AAAAAG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18596548_18596552dup , CM000681.2:g.18596548_18596552dup	GRCh38
NC_000019.9:g.18707358_18707362dup , CM000681.1:g.18707358_18707362dup	GRCh37
NC_000019.8:g.18568358_18568362dup	NCBI36
NG_013370.1:g.15308_15312dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684169.1:c.1024+79_1024+83dup	ENSP00000506849.1:n.1024+79_1024+83dup
ENST00000392386.8:c.1024+79_1024+83dup MANE Select	ENSP00000376188.2:n.1024+79_1024+83dup
ENST00000392386.7:c.1024+79_1024+83dup	ENSP00000376188.2:n.1024+79_1024+83dup
ENST00000597131.1:c.447+121_447+125dup
NM_004750.4:c.1024+79_1024+83dup	NP_004741.1:n.1024+79_1024+83dup
XM_011528422.1:c.958+79_958+83dup	XP_011526724.1:n.958+79_958+83dup
XM_011528423.1:c.1024+79_1024+83dup	XP_011526725.1:n.1024+79_1024+83dup
XM_011528424.1:c.958+79_958+83dup	XP_011526726.1:n.958+79_958+83dup
XM_011528422.2:c.958+79_958+83dup	XP_011526724.1:n.958+79_958+83dup
XM_011528423.2:c.1024+79_1024+83dup	XP_011526725.1:n.1024+79_1024+83dup
XM_011528424.3:c.958+79_958+83dup	XP_011526726.1:n.958+79_958+83dup
NM_004750.5:c.1024+79_1024+83dup MANE Select	NP_004741.1:n.1024+79_1024+83dup